American Diagnostica, Inc.
2 FDA 510(k) clearances · Recalling firm
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| Record | Firm | Date |
|---|---|---|
| REF 822 IMUBIND(R) Plasma PAI-1 ELISA The intended use: Product is an enzyme-linked immuno recall (Z-1426-2010) | American Diagnostica, Inc. | 2010-04-21 |
| American Diagnostica Inc. ACTICLOT dPT Reference 824 in vitro diagnostic recall (Z-0779-2007) | American Diagnostica, Inc. | 2007-05-03 |
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Every clearance here is in the API, with alerts when new ones post.